1462351-55-8

Basic information

• Product Name: (1S,2S,5R)-(+)-neomenthyl selenol
• Synonyms: (1S,2S,5R)-(+)-neomenthyl selenol
• CAS NO: 1462351-55-8
• Molecular Weight: 219.229
• Mol File: 1462351-55-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1S,2S,5R)-(+)-neomenthyl selenol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,5R)-(+)-neomenthyl selenol(1462351-55-8)
• EPA Substance Registry System: (1S,2S,5R)-(+)-neomenthyl selenol(1462351-55-8)

Safety Data

• Hazardous Substances Data: 1462351-55-8(Hazardous Substances Data)

Upstream product

• 2216-52-6 Neomenthol 
• 2230-82-2 (1S,2S,5R)-(+)-2-isopropyl-5-methylcyclohexyl tosylate 
• 910660-22-9 (+)-dineomenthyl diselenide 
• 2230-82-2 menthyl tosylate 
• 2216-51-5 (-)-menthol 

Downstream Products

• 1462351-64-9 (1S,2S,5R)-(+)-(E)-cinnamyl neomenthyl selenide 
• 1462351-65-0 (1S,2S,5R)-(+)-(Z)-cinnamyl neomenthyl selenide 
• 1462351-66-1 (1S,2S,5R)-(+)-geranyl neomenthyl selenide 
• 1462351-67-2 (1S,2S,5R)-(+)-neomenthyl neryl selenide 
• 104713-12-4 (R)-1-phenylprop-2-en-1-ol 
• 104713-12-4 (1S)-1-phenylprop-2-en-1-ol 
• 910660-22-9 (+)-dineomenthyl diselenide 

Relevant articles and documents

Chirality transfer through sulfur or selenium to chiral propellers

The mechanism of chirality transfer from a chiral alkyl substituent to a trityl moiety through sulfur or selenium atoms is analysed and discussed on the basis of ECD measurements, DFT structure and ECD spectra calculations. It is shown that the presence o

Synthesis and reactions of the optically active selenols derived from monoterpenes Dedicated to Professor Jacek Gawronski on the occasion of his 70th birthday

A convenient methodology for the synthesis of optically active selenols, derived from p-menthane, carane, and pinane, is described. The selenols were oxidized with air to give the optically active diselenides, and were also converted into the corresponding allylic selenides via reaction with Z- and E-cinnamyl, geranyl, and neryl chlorides. Oxidation of the allylic selenides with mCPBA gave the optically active alcohols via [2,3]-sigmatropic rearrangement of the in situ generated allylic selenoxides.